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NCT07610538Recruiting

Low-dose Interleukin-2 After Myocardial Infarction to Investigate Effects on Tissue-resident Regulatory T Cells

Source: ClinicalTrials.gov · Last updated 28 May 2026

Brief summary (registry, in English)

The primary goals of this study are to compare the differences in tissue-resident Treg gene signature for activation, proliferation, and suppressive function using single-cell/-nucleus RNA sequencing in patients treated with ld-IL-2 compared to control grouped by individual tissue beds from in and around the heart. Additionally, tissue-resident Tregs will be compared to peripheral blood Tregs from the same patient to assess the differential effect of ld-IL-2 on the two compartments.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
24 (estimated)
First submitted
20 May 2026
Start date
31 Mar 2026
Primary completion date
1 Nov 2028
Lead sponsor
Cambridge University Hospitals NHS Foundation Trust
NCT number
NCT07610538

What you commit to

  • Study type: Interventional
  • Planned participants: 24
  • From 31 Mar 2026 to the primary completion date, 1 Nov 2028
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any regular immunosuppressive treatment \[Inhaled or topical steroids are permissible\]
  • Vaccine within 4 weeks prior to screening

Other illness

  • Critical left main stem coronary disease
  • Severe valvular disease (for example 'severe' aortic stenosis as classified on echocardiogram report)
  • Haemodynamic instability caused by arrhythmia requiring cardioversion in the current admission
  • Autoimmune disease
  • Allergy or intolerance to aldesleukin
  • Signs and symptoms of active infection
  • History of human immunodeficiency virus (HIV), hepatitis B or C
  • Current malignancy requiring active treatment
  • Clinically relevant medical or surgical conditions that, in the opinion of the investigator, would put the subject at risk by participating in the study

Lab values

  • Known active hepatic disease or alanine aminotransferase (ALT) \> 3xULN
  • Severe chronic kidney disease (defined as eGFR \< 30 ml/min/1.73m2)

Age

  • Women of child-bearing potential and pregnancy (women must be either postmenopausal (defined as being amenorrhoeic for greater than 2 years with an appropriate clinical profile (e.g. age appropriate (\>55 years old), history of vasomotor symptoms) or having documented hysterectomy and/or bilateral oophorectomy)

Other

  • Non-sustained ventricular tachycardia of \>10 beats in the last 48 hours
  • Women who are breast-feeding

Who the study is looking for

  • Aged over 18 years old
  • Undergoing CABG surgery

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Royal Papworth Hospital NHS Foundation Trust
Coordinator of this site? Confirm its status
CambridgeUnited KingdomRecruiting
Addenbrooke's Hospital
Coordinator of this site? Confirm its status
CambridgeUnited KingdomRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.